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1 Section of Cardiovascular Sciences, Department of Medicine, Baylor College of Medicine, Houston 77030; 2 Indus Instruments, Houston, Texas 77058; and 3 Department of Pharmacology, Berlex Biosciences, Richmond, California 94804
Apolipoprotein E-knockout (ApoE-KO) mice develop advanced
atherosclerotic lesions by 1 yr of age and have been well characterized pathologically and morphologically, but little is known regarding their
cardiovascular physiology and hemodynamics. We used noninvasive Doppler
ultrasound to measure aortic and mitral blood velocity and aortic
pulse-wave velocity in 13-mo-old ApoE-KO and wild-type (WT) mice
anesthetized with isoflurane. In other mice from the same colony, we
measured systolic blood pressure, body weight, heart weight,
cholesterol, and hematocrit. Heart rate and blood pressure were
comparable (P = not significant) between ApoE-KO and WT
mice, but significant decreases (P < 0.001) were found in body weight (
22%) and hematocrit (
11%), and significant
increases were found in heart weight (+23%), aortic velocity (+60%),
mitral velocity (+81%) (all P < 0.001), and
pulse-wave velocity (+13%, P < 0.05). We also found
inflections in the aortic arch velocity signal consistent with enhanced
peripheral wave reflection. Thus ApoE-KO mice have phenotypic
alterations in indexes of peripheral vascular resistance and compliance
and significantly elevated cardiac outflow velocities and heart
weight-to-body weight ratios.
atherosclerosis; cardiac output; hypertrophy; ultrasonics
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